Ilahi Amin, Hadrich Inès, Neji Sourour, Trabelsi Houaida, Makni Fattouma, Ayadi Ali
Fungal and Parasitic Molecular Biology Laboratory, Faculty of Medicine, University of Sfax, Rue Magida Boulila, Sfax, 3029, Tunisia.
Curr Microbiol. 2017 Jun;74(6):671-677. doi: 10.1007/s00284-017-1237-7. Epub 2017 Mar 22.
Lipophilic yeast Malassezia species is widely found on the skin surface of humans and other animals. This fungus can cause pityriasis versicolor, Malassezia folliculitis, and seborrheic dermatitis. Still now, there is a problem with species identification of Malassezia with conventional methods. We developed a real-time polymerase chain reaction (PCR) assay with multiple hybridization probes for detecting M. globosa, M. furfur, M. restricta, M. sympodialis, M. slooffiae, and M. pachydermatis. The amplification curves and specific melting peaks of the probes hybridized with real-time PCR product were used for species identifications. The assay was further evaluated on 120 samples which were performed by swabbing from 60 domestic animals (23 goats, 10 dogs, 15 cows, 3 cats, 8 rabbits, and 1 donkey) and in 70 human samples (28 patients with pityriasis versicolor, 17 breeders, and 25 control group). Fifteen M. pachydermatis were identified from animals. From human, 61 isolates were identified as M. globosa (28), M. furfur (15), M. restricta (6), M. sympodialis (8), M. slooffiae (2), and M. pachydermatis (2). Eight cases of co-detection from 6 patients and 2 breeders were revealed. Our findings show that the assay was highly effective in identifying Malassezia species. The application of multiplex real-time PCR provides a sensitive and rapid identification system for Malassezia species, which may be applied in further epidemiological surveys from clinical samples.
亲脂性酵母马拉色菌属广泛存在于人类和其他动物的皮肤表面。这种真菌可引起花斑糠疹、马拉色菌毛囊炎和脂溢性皮炎。目前,用传统方法对马拉色菌进行菌种鉴定存在问题。我们开发了一种带有多个杂交探针的实时聚合酶链反应(PCR)检测方法,用于检测球形马拉色菌、糠秕马拉色菌、限制性马拉色菌、合轴马拉色菌、斯洛菲马拉色菌和厚皮马拉色菌。与实时PCR产物杂交的探针的扩增曲线和特异性熔解峰用于菌种鉴定。该检测方法在120份样本上进一步评估,这些样本是通过擦拭60只家畜(23只山羊、10只狗、15头牛、3只猫、8只兔子和1头驴)和70份人类样本(28例花斑糠疹患者、17名饲养员和25名对照组)获得的。从动物样本中鉴定出15株厚皮马拉色菌。从人类样本中,61株分离株被鉴定为球形马拉色菌(28株)、糠秕马拉色菌(15株)、限制性马拉色菌(6株)、合轴马拉色菌(8株)、斯洛菲马拉色菌(2株)和厚皮马拉色菌(2株)。发现6例患者和2名饲养员中有8例为共同检测。我们的研究结果表明,该检测方法在鉴定马拉色菌种方面非常有效。多重实时PCR的应用为马拉色菌种提供了一种灵敏、快速的鉴定系统,可应用于临床样本的进一步流行病学调查。